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For Companies At a Glance
- Tasks: Lead clinical trials in oncology, ensuring patient safety and regulatory compliance.
- Company: Join GSK, a global biopharma leader with a mission to impact 2.5 billion lives.
- Benefits: Full-time role with opportunities for growth in a dynamic environment.
- Other info: Collaborative culture focused on innovation and patient outcomes.
- Why this job: Make a real difference in cancer treatment while working with cutting-edge science.
- Qualifications: Bachelor's degree in Life Science and 2+ years of clinical trial experience required.
The predicted salary is between 36000 - 60000 £ per year.
Overview
GSK Greater London, England, United Kingdom
Join to apply for the Director, Clinical Scientist- Oncology role at GSK
Site Name: USA – Massachusetts – Waltham, Switzerland – Zug, UK – United Kingdom, Upper Providence, Warsaw
Posted Date: Sep 16 2025
Director Clinical Scientist- Oncology
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
Responsibilities
- The Director, Clinical Scientist, Oncology has accountability for providing clinical input during protocol development, oversight of study conduct, and interpretation of study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted patient population.
- Lead a clinical matrix team and ensure patient safety is of paramount importance during the study lifecycle; ensure study objectives fulfil regulatory and reporting requirements; support medical governance through the Medical Director and/or the Clinical Development Lead and other Study Team members/stakeholders.
- Design and execute, in collaboration with the Medical Director, the clinical trial(s) assigned to the project; engage and influence a diverse scientific community of internal and external experts, including collaborations; may manage other staff within Clinical Sciences.
- Note: This position requires on-site presence 2 to 3 days a week in the UK (London or Stevenage); Switzerland (Zug); US (Upper Providence, PA; Waltham, MA or Boston, MA); or Poland (Warsaw).
Accountabilities
- Accountable for Phase 1-4 study design, including clinical pharmacology study designs supporting the CDP
- Understand objectives around safety, efficacy, endpoints, biology, pharmacology, toxicology, biomarkers, and data-driven phenotypes
- Author the Clinical Study Proposal (CSP), prepare and present the study at Protocol Review Forum (PRF), and incorporate governance feedback
- Ensure study protocol reflects input from internal and/or external experts and thought leaders
- Collaborate with functions to ensure the study evaluates key aspects of the Asset Product Profile
- Provide input into regulatory documents and ensure timely regulatory reporting
- Lead or participate in regulatory interactions and ensure quality communications with study sites
- Interpret study data for clinical study reports (CSRs) and regulatory submissions; ensure input from experts is reflected
- Communicate results to internal/external stakeholders and regulators
- Drive content of clinical documents (e.g., Investigator Brochure) and regulatory documents (DSURs, BRMP, DCSI, Annual Safety Reports, PBRs)
- Lead completion/filing of key components of clinical modules for regulatory submissions
- Prepare and present data for external dissemination (abstracts, posters, conference presentations)
- Engage in advisory boards and scientific engagement activities; deliver end-of-study reports
Qualifications
Basic Qualifications
- Bachelor’s degree in Life Science or equivalent
- 2+ years of pharma industry or relevant clinical trial experience
- 2+ years of clinical trial and clinical research experience; running clinical trials in early or late phases
- Experience in a matrix management and large cross-functional team environment
- Experience generating clinical Protocols and ICFs
- Experience working with data management and data cleaning of clinical data
Preferred Qualifications
- Advanced degree (e.g., MS, PhD, PharmD, RN) or equivalent experience
- Oncology or immuno-oncology experience preferred
- Ability to build internal and external relationships in a dynamic, matrixed environment
- Strong communication skills tailored to the audience; good knowledge of disease-specific research priorities and regulatory landscape
- Broad understanding of pharmaceutical development and regulatory requirements
- Demonstrated leadership in cross-functional clinical development and program delivery
- Experience across study, project, and program levels; ability to work across multiple projects
- Awareness of business drivers and alternative delivery solutions; strong interpersonal skills
- Knowledge of worldwide regulatory and safety requirements; experience leading in matrix and line environments
Why GSK
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases. We are committed to creating an environment where our people can thrive and focus on what matters most.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre for accessibility support.
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, pregnancy, gender identity, sexual orientation, parental status, national origin, age, disability, genetic information, military service or any basis prohibited under law.
Seniority level
- Not Applicable
Employment type
- Full-time
Job function
- Health Care Provider
- Industries: Pharmaceutical Manufacturing
Note: Referrals may not be required to apply; information regarding benefits may be provided by the employer as part of recruitment communications.
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Director, Clinical Scientist- Oncology employer: Gsk
Contact Detail:
Gsk Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director, Clinical Scientist- Oncology
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at GSK or in oncology. A friendly chat can open doors and give you insider info that could help you stand out.
✨Tip Number 2
Prepare for interviews by diving deep into GSK's recent projects and breakthroughs in oncology. Show us you’re not just another candidate; demonstrate your passion and knowledge about their mission to impact patient health.
✨Tip Number 3
Practice your pitch! Be ready to explain how your experience aligns with the role of Director, Clinical Scientist. We want to hear how you can lead clinical trials and ensure patient safety while meeting regulatory requirements.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find all the latest roles and updates directly from GSK.
We think you need these skills to ace Director, Clinical Scientist- Oncology
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Director, Clinical Scientist- Oncology role. Highlight your relevant experience in clinical trials and oncology, and show us how your skills align with our mission at GSK.
Showcase Your Achievements: Don’t just list your responsibilities; we want to see your impact! Use specific examples of how you've contributed to successful clinical trials or improved patient outcomes in your previous roles.
Be Clear and Concise: Keep your application straightforward and to the point. We appreciate clarity, so avoid jargon and ensure your key points stand out. This will help us quickly see why you’re a great fit for the team!
Apply Through Our Website: We encourage you to submit your application directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining GSK.
How to prepare for a job interview at Gsk
✨Know Your Oncology Stuff
Make sure you brush up on the latest trends and breakthroughs in oncology. GSK is looking for someone who can engage with a diverse scientific community, so being well-versed in current research and clinical practices will definitely give you an edge.
✨Showcase Your Leadership Skills
As a Director, you'll be leading a clinical matrix team. Be prepared to discuss your experience in managing cross-functional teams and how you've successfully driven projects forward. Use specific examples to illustrate your leadership style and impact.
✨Understand Regulatory Requirements
Familiarise yourself with the regulatory landscape relevant to clinical trials. GSK values accountability and compliance, so demonstrating your knowledge of regulatory processes and your experience in preparing documents like Clinical Study Proposals will be crucial.
✨Communicate Effectively
Strong communication skills are key for this role. Practice articulating complex scientific concepts in a way that's easy to understand. Think about how you would present study results to different stakeholders, as this will show your ability to tailor your message to your audience.